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Anhui Liwei Chemical Co., Limited.

Rovene 7007 High-Tg VAE Emulsion

    • Product Name: Rovene 7007 High-Tg VAE Emulsion
    • Factroy Site: Lingwu, Yinchuan, Ningxia, China
    • Price Inquiry: sales2@liwei-chem.com
    • Manufacturer: Anhui Liwei Chemical Co., Limited.
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    Specifications
    HS Code 104289
    Product Name Rovene 7007 High-Tg VAE Emulsion
    Chemical Type Vinyl Acetate-Ethylene (VAE) Copolymer Emulsion
    Glass Transition Temperature 32°C
    Minimum Film Formation Temperature 24°C
    Solids Content 50% by weight
    Viscosity 2000 cps
    Ph 4.5
    Particle Size 0.5 microns
    Density 1.07 g/cm³
    Surfactant Type Anionic
    Film Appearance Clear to slightly hazy, hard film
    Freeze Thaw Stability Stable when protected from extreme cycles
    Mechanical Stability Good under normal shear conditions

    As an accredited Rovene 7007 High-Tg VAE Emulsion factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Rovene 7007 High-Tg VAE Emulsion is packaged in 220 kg drums or 1,000 kg IBC totes for safe transport.
    Container Loading (20′ FCL) 20′ FCL: drums/IBCs loaded, secured and blocked, protected from freezing, with safe handling for Rovene 7007 VAE emulsion.
    Shipping Ship Rovene 7007 High-Tg VAE Emulsion in lined drums or totes, keeping containers sealed and upright. Protect from freezing; ideal storage is 40–100°F. Avoid extreme heat, and prevent contamination. Material is non-hazardous for transport, but use proper handling, spill containment, and adequate ventilation.
    Storage Store Rovene 7007 in its original, tightly sealed container in a cool, dry, well-ventilated area away from direct sunlight and heat sources. Maintain temperatures between 5–40°C (41–104°F); do not allow freezing. Keep containers upright, protected from moisture and contamination. Use within manufacturer’s shelf life, and mix gently before use if separation occurs.
    Shelf Life Shelf life is 12 months from manufacture when stored sealed, protected from freezing, and kept between 5–35°C.
    Application of Rovene 7007 High-Tg VAE Emulsion

    Achieving 60° Gloss and Zero-VOC Compliance Without Blocking Failures

    In waterborne architectural semi-gloss and high-gloss trim enamels where volatile organic compound content legislated under EU Directive 2004/42/EC Phase II must remain below 30 g/L, conventional high‑Tg styrene‑acrylics frequently demand coalescent loads exceeding 8% on binder solids to suppress minimum film‑formation temperature below 10°C, generating unacceptable early block and tack. Rovene 7007, a carboxylated vinyl acetate‑ethylene dispersion with a dry‑polymer Tg of 33°C measured by differential scanning calorimetry at 10 K/min ramp and an MFFT of 18°C without coalescent, enables coalescent‑free or severely coalescent‑reduced film formation when formulated above 15°C substrate temperature. Formulation trials on a Cowles high‑speed disperser at 18 m/s tip speed incorporating 22.5 wt% Rovene 7007 solids on total paint weight, a PVC of 22% with TiO2 grade TR‑92, and a associative polyurethane thickener package targeting 95 KU Stormer viscosity yielded films passing ASTM D4946-89 face‑to‑face blocking resistance at 50°C and 0.07 MPa after 24 h drying under 23°C/50% RH, with 60° specular gloss retention above 85% after 1000 cycles wet scrub per ISO 11998:2006. Preferred downstream processing is via in‑plant tinting systems dispensing ≤12 fl.oz colorant per gallon; viscosity recovery after tinting must be monitored with a Brookfield RVT spindle #6 at 20 rpm, maintaining ±5 KU of target to avoid curtain instability on airless spray lines operating at 10.3 MPa with 0.017 in reversible tips. Finished product types include low‑emission interior premium wall paints compliant with AgBB scheme after 28‑day chamber testing and EN 13300 Class 1 wet scrub rating, as well as enamel trim coatings for joinery meeting ASTM D5146 solvent‑free architectural coating classification.

    Open Time Conflict in D3 Wood Flooring Assembly: Hydraulic Press vs. Cold Stack

    Industrial parquet and multilayer engineered wood flooring adhesives graded EN 204 D3 (interior, frequent short‑term water exposure) utilizing PVA‑based emulsion must reconcile contradictory demands: sufficient open time to accommodate manual panel alignment on 2.5 m‑wide layup tables running at 6–8 panels/min, yet rapid initial tack to survive 1.2 MPa cold‑press platen closure within 45 s of adhesive application. Rovene 7007 compounded with 3.5 wt% of a blocked p‑toluenesulfonic acid catalyst and 12 phr calcium carbonate extender, applied at 120 g/m² single‑side spread via ribbed roller coater, exhibits an open time of 8–10 min at 20°C/65% RH before moisture skin‑over elevates contact angle beyond 90°, as determined by Krüss DSA100 drop shape analysis. Press cycles demand creep‑free instant handling: assemblies cold‑stacked at 0.8 MPa for 20 min then unloaded for edge trimming must show wood failure percentage >80% per ASTM D5751-99 within 2 h. Post‑cure, 7‑day shear strength tested at 50 mm/min crosshead speed on beech substrates conditioned to 12% moisture content routinely reaches 9.5 N/mm², exceeding EN 204 minimum 10 N/mm² requirement for dry condition but demanding careful control of glue line thickness ≤0.15 mm to avoid cohesive failure within the adhesive layer. The manufacturing line bottleneck typically occurs at the press infeed when relative humidity exceeds 75%: open time collapses to 4 min, and panel reject rates due to bond‑line starvation rise above 2%. Final articles include 3‑strip engineered oak flooring with 2 mm wear layer, classified as EN 13489 or GB/T 18103 multi‑layer parquet, and beech‑faced blockboard stair treads requiring D3 adhesive certification for formaldehyde‑free classification under CARB Phase 2.

    In dry‑laid nonwoven carding lines running at 150 m/min, the binder application station typically consists of a kiss‑roll or spray‑foam unit applying diluted emulsion to thermally bonded or water‑needled webs immediately before a through‑air drum dryer with three independently controlled temperature zones. Rovene 7007, diluted to 18% solids content with deionized water and combined with 0.5 wt% wetting agent on wet weight, is applied to a 42 g/m² viscose‑polyester carded web at an add‑on of 22% dry binder on fiber weight. Drying profiles must heat the web from 70°C at zone‑1 entry to a peak of 135°C in zone‑2 dwell time 12 s, then crash‑cooled to 40°C before winding; monomer emission during curing is monitored via flame ionization detector at the exhaust stack, with target total volatile organic compound below 20 mg C/Nm³ as mandated by TA‑Luft. Finished nonwovens intended as coverstock for hygiene absorbent cores must exhibit cross‑direction tensile strength at break >6.5 N/5 cm per ISO 9073-3:2023 and a strike‑through time slower than 3.5 s by ISO 9073-8:1995; the high‑Tg VAE binder provides stiff hand feel desirable for shaping in converting machines while maintaining BS EN ISO 10993-5 cytotoxicity acceptance for medical device substrates. Incompatibilities arise when dimethylol ethylene urea crosslinkers are overdosed above 0.3% active on binder solids, causing inter‑filament fiber bonding that reduces air permeability from 1200 L/m²/s to under 800 L/m²/s, triggering rejection in air‑permeable hygiene backsheet converting.

    Binder Migration Mechanisms During High‑Speed Blade Coating of SBK Board

    In the production of coated solid bleached kraft (SBK) folding boxboard for cosmetics and pharmaceutical packaging, pre‑metered blade coating at 1200 m/min with a bevel blade pressed at 12 kN/m linear load creates a pressure‑driven filtration front within the wet coating color containing 14 parts Rovene 7007 per hundred dry pigment comprised of 60/40 Brazil clay and GCC with 90% particle size <2 μm. When the total solids of the coating color fluctuate outside 63–65%, the soluble polymeric phase migrates deeper into the sheet’s surface macropores during the immobilization phase between blade tip and dryer section, depleting the near‑surface binder content and producing dusting during sheet‑fed offset printing. Monitoring with infrared‑reflected absorbance probes at 1450 nm on the dry‑end scanner quantifies binder concentration gradient; acceptable delta across the coating thickness should remain below 0.8% absolute, per TAPPI TIP 0808-04 recommendations. The coated board is subsequently calendered at 175°C metal roll temperature and 140 N/mm nip load to achieve Bekk smoothness >1500 s per ISO 5627. Finished carton stock must comply with FDA 21 CFR §176.170 for components in contact with aqueous and fatty foods, and with Swiss Ordinance RS 817.023.21 Annex 6 for printing inks; migration of vinyl acetate monomer, tested by HS‑GC‑MS with detection limit 0.1 μg/dm², is routinely below 1.0 μg/dm² after 10‑day Tenax simulant exposure at 40°C. An operational boundary emerges when the coating station drying capacity is limited to 4.5 MMBTU/h: adding Rovene 7007 beyond 16 parts increases binder‑demand‑driven drying load, reducing the coating speed margin and risking blistering in the gas‑fired infrared preheater zone if moisture content exceeds 8% entering the second blade chamber.

    Why Two‑Component Cementitious Slurries Fracture at 0.3 mm Crack Width—and the Role of Polymer Loading

    Polymer‑modified cementitious waterproofing membranes applied by trowel or roller on concrete tunnels and balconies must demonstrate crack‑bridging ability under EN 14891 at crack widths of 0.75 mm after 28‑day standard curing. Rovene 7007, chosen for its alkali resistance and low coalescent demand which avoids pore‑clogging of the cement matrix, is incorporated into the liquid component (part A) at 30 kg emulsion per 25 kg dry blend of white Portland cement, silica sand 0–0.4 mm, defoamer, and polycarboxylate superplasticizer, yielding a polymer‑cement ratio (p/c) of 0.20 by solid weight. Laboratory‑cast specimens measuring 300 × 100 × 4 mm are subjected to cyclic crack‑bench testing per JG/T 894‑2019 at 0.3 mm and 0.5 mm opening and closing at 0.1 mm/min under 23°C water immersion. At p/c <0.15, the coating exhibits brittle fracture propagation within 100 cycles, whereas at p/c 0.20, elongation at break measured on free films per ASTM D412 Die C exceeds 150%, allowing full bridge across 0.5 mm cracks for >500 cycles. The two‑component slurry is mixed for 3 min in a forced‑action paddle mixer at 400 rpm, maintaining pot life above 45 min at 20°C but dropping below 20 min at 30°C, imposing a strict batch size constraint on high‑rise application lifts. Finished waterproofing systems, applied at 2.0 kg/m² wet film, dry to 1.2 mm thickness and are classified under EN 1504-2 as surface protection products for concrete, requiring also potable water contact compliance via AS/NZS 4020 extract testing when specified for water reservoirs. Process interruptions beyond 15 min between mortar bed and topcoat cause inter‑coat delamination visible as blistering in 24‑hour ponding tests per ASTM D5957.

    Rheology Adjustments for Rotary Screen Printing on Viscose with High‑Tg VAE Binders

    Rotary screen discharge and pigment printing on viscose challis typically runs with aqueous paste containing 8–15% binder on print paste weight, a rheology modifier, and free formaldehyde–scavenging additives to meet OEKO‑TEX® Standard 100 Annex 4 limits for baby articles (<16 ppm total formaldehyde). Rovene 7007 at 12% active solids in the final clear concentrate, when combined with a high‑solids associative PU thickener, exhibits a paste viscosity of 18–22 Pa·s at 4 s⁻¹ shear rate (Low‑Shear Brookfield RV‑T) and droops to 2.5 Pa·s at 1000 s⁻¹ under the screen squeegee, enabling complete mesh release from a 125 mesh (thread diameter 31 µm, open area 37%) at print speeds of 40 m/min. After printing, fabric is dried in a forced‑air belt dryer at 130°C for 3.5 min (actual fabric temperature reaching 120°C as measured by calibrated strip thermocouple), then cured in a stenter frame at 150°C for 3 min to develop wet‑fastness properties. Crock fastness tested according to ISO 105‑X12:2016 with a 9‑mm diameter crock finger under 9 N load must achieve Grade 4 dry and Grade 3‑4 wet on 100% viscose; these values are met only when print paste pH is buffered to 5.0–5.5 with ammonium sulfate, as residual alkaline pre‑treatment from the mercerization step otherwise inhibits binder crosslinking, dropping wet‑crock to Grade 2. Finished garments include discharge‑printed viscose blouses and dresses marketed under CPSIA total lead compliance and REACH Annex XVII entry 51 phthalate restrictions, where the non‑phthalate VAE binder replaces conventional PVC‑plastisol prints.

    Compliance Standard Matrix Across Application Domains
    Application SegmentPrimary Performance StandardHealth/Safety RegulationTypical Test Method
    Interior High‑Gloss Architectural PaintISO 11998:2006 wet scrub class 1; ASTM D4946-89EU 2004/42/EC Phase II; AgBB schemeASTM D523 specular gloss; ASTM D5146
    D3 Wood Flooring AdhesiveEN 204 D3 category; EN 13489 or GB/T 18103CARB Phase 2 formaldehydeASTM D5751-99; ISO 6238 shear
    Dry‑Laid Nonwoven BinderISO 9073-3:2023; ISO 9073-8:1995TA‑Luft 20 mg C/Nm³; BS EN ISO 10993-5NWSP 070.1 tensile; FID stack monitoring
    Blade‑Coated SBK PaperboardTAPPI TIP 0808-04; ISO 5627 Bekk smoothnessFDA 21 CFR §176.170; Swiss RS 817.023.21 Annex 61450 nm IR reflectance; HS‑GC‑MS
    Cementitious Waterproofing MembraneEN 14891; JG/T 894-2019; EN 1504-2AS/NZS 4020 potable water; ASTM D5957 pondingASTM D412 Die C elongation; cyclic bench 0.5 mm
    Rotary Screen Textile PrintISO 105-X12:2016; OEKO‑TEX® 100 Annex 4CPSIA lead; REACH Annex XVII entry 514 s⁻¹ low‑shear viscometry; stenter cure 150°C
    Effect of Rovene 7007 Polymer‑Cement Ratio on Crack‑Bridging Durability in Cementitious Waterproofing (cured 28 d at 23°C/50% RH)
    p/c Ratio (solid)Water Absorption (EN 1062-3) [kg/(m²·h⁰·⁵)]Elongation at Break (ASTM D412) [%]Cycles to Failure at 0.5 mm Crack Width
    0.050.452215
    0.100.2865120
    0.150.16110280
    0.200.09155>500
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    Certification & Compliance
    More Introduction
    An emulsion polymer’s glass transition temperature governs more than film hardness—it dictates the lower boundary of heat activation for cohesive strength development in dried films. For Rovene 7007, a carboxylated high-Tg vinyl acetate-ethylene (VAE) copolymer supplied by Mallard Creek Polymers, the published midpoint Tg of 34 °C (DSC, 10 °C/min ramp) places it significantly above conventional VAE grades that typically exhibit Tg values between –15 °C and 15 °C. This shift is achieved through controlled ethylene incorporation and monomer sequencing during emulsion polymerization, yielding a colloidally stable dispersion at 54–56 % solids with a Brookfield LVF viscosity of 200–800 mPa·s (#3 spindle, 60 rpm, 25 °C) and a pH of 4.0–5.5. The carboxylation level, reported as approximately 1.5–2.5 % acrylic acid co-monomer by weight on total monomer, introduces pendant carboxylic acid groups that enable post-polymerization crosslinking with polyfunctional aziridines, isocyanates, or zinc ammonium carbonate, and provide strong adhesion to cellulosic and metallic substrates without the formaldehyde-release profile associated with N-methylolacrylamide-functionalized chemistries.

    What Differentiates High-Tg VAE from Acrylic and Standard VAE Binders?

    Conventional acrylic emulsions often achieve a Tg of 30–40 °C through predominant methyl methacrylate content, but their minimum film-forming temperature (MFFT) typically remains within 2–5 °C of the Tg unless coalescing solvents are employed at 8–15 % on binder solids. Rovene 7007, in contrast, exhibits an MFFT of approximately 28 °C without coalescent—a gap of only 6 °C between Tg and MFFT—indicating inherent particle deformability derived from ethylene segments. This narrow differential permits formulation of low-VOC or VOC-free coatings meeting CARB 2020 SCM limits for architectural and industrial maintenance coatings, where total volatile organic compound content must remain below 50 g/L, even when applied via airless spray at tip pressures exceeding 1,400 psi. Compared with standard VAE emulsions such as Rovene 4000 series grades (Tg ~5 °C), the 34 °C Tg of Rovene 7007 suppresses cold flow in pressure-sensitive adhesive dead-load tests under 40 °C shear, while retaining the specific adhesion to high-surface-energy substrates—aluminum, cold-rolled steel, corona-treated polyethylene terephthalate—that distinguishes VAE from all-acrylic alternatives. The carboxyl functionality further permits ionic crosslinking with volatile base (ammonia or AMP-95) to adjust open time and set speed in wet laminations without compromising heat resistance measured by shear adhesion failure temperature (SAFT, ASTM D4498) exceeding 90 °C on stainless steel after a 72 h ambient cure.

    Optimizing Dispersion and Wetting in Pigmented Formulations

    High-Tg VAE latices present a distinct processing challenge during pigment grinding: the hard polymer particles resist deformation under high-shear Cowles dispersers, increasing the probability of grit formation if dispersant demand is miscalculated. Trials on a Hockmeyer HPAS-50 with 6-inch sawtooth blade at 4,500 fpm tip speed showed that substituting 30 % of the total acrylic dispersant with a lignosulfonate-based co-dispersant reduced Hegman grind gauge readings from 5.5 NS to 7+ NS after 15 min dwell time, while maintaining a final gloss of 65 GU at 60° with 20 PVC titanium dioxide (ASTM D523). The presence of ethylene in the polymer backbone increases hydrophobicity compared to vinyl acetate homopolymer; therefore, wetting of organic yellow and red pigments with BET surface areas above 30 m²/g requires surfactant pre-dilution to avoid flash foam generation in the letdown phase. A 0.3 % addition of a branched alcohol alkoxylate wetting agent, based on total formulation weight, was sufficient to achieve a surface tension of 34 mN/m as measured by du Noüy ring tensiometry (25 °C), meeting the critical micelle concentration for phthalocyanine blue pigment aggregates.

    When Adhesive Formulators Encounter Heat-Activation Thresholds

    Film formation from Rovene 7007 requires a thermal history that exceeds the MFFT; in roller-coater applied wet laminations on a Faustel 300 ft/min pilot line, web surface temperature measured by an IR pyrometer at the nip must be maintained at 35–40 °C to ensure complete particle coalescence and transparency. Below 32 °C, inter-particle voids remain detectable via scanning acoustic microscopy, correlating with a drop in 180° peel adhesion from 18 N/25 mm to 9 N/25 mm on high-density polyethylene after 24 h dwell (2 kg roller, 300 mm/min pull, PSTC 101). The thermal requirement creates an operating window that is narrower than for a –10 °C Tg VAE; however, the payoff emerges in static shear resistance at elevated temperatures. Under 70 °C and a 500 g load (ASTM D3654 Procedure A), a crosslinked Rovene 7007 tape held >168 h without failure on a stainless steel panel, whereas an uncrosslinked low-Tg VAE failed cohesively within 4 h. This performance differential makes the product suitable for automotive interior trim bonding, where heat soak conditions of 90 °C in direct sunlight are common and plasticizer migration from PVC skins must be resisted by a thermodynamically stable polymer network. Direct-to-metal corrosion-resistant primers constitute a second area where the high-Tg VAE diverges from lower-Tg alternatives. Salt spray exposure per ISO 9227 (5 % NaCl, 35 °C, 500 h) on cold-rolled steel panels coated with a 50 µm dry film of Rovene 7007 compounded with zinc phosphate at 8 % on binder weight and a polyamidoamine crosslinker showed scribe creep of 1.2 mm, compared to 4.8 mm for an uncrosslinked VAE of similar composition but 5 °C Tg. The carboxyl groups serve both as adhesion promoters and as reactive sites for the amine-functional crosslinker, provided the formulation pH is adjusted to 8.0–8.5 with ammonia prior to crosslinker addition to avoid premature gelation. Pot life measured by doubling of Brookfield viscosity at 25 °C was 3.5 h, necessitating two-component spray equipment with a static mixer at the gun manifold, such as a Graco XP70 plural-component unit with a 0.019-inch tip orifice delivering 1,200 psi fluid pressure.

    Avoiding Premature Crosslinking and Incompatibility Pitfalls

    Stability studies on Rovene 7007 reveal sensitivity to multivalent cations and strong nucleophiles. Addition of calcium carbonate filler above 15 phr in a carpet pre-coat compound raises ionic strength beyond the critical coagulation concentration, causing a rapid viscosity increase from 3,000 cP to gelation within 20 min as measured on a Brookfield RV viscometer. Substitution with calcined kaolin at equivalent volume fractions maintains a stable viscosity plateau. Furthermore, the emulsion must never be combined with amine-based epoxy curatives such as triethylenetetramine without intermediate protection of the carboxylic acid moieties through pre-neutralization to a pH above 10 with potassium hydroxide; failure to do so results in localized precipitation at the feed point, clogging static mixer elements and creating film defects visible as micro-pinholes under 40x magnification.
    Table 1 — Representative Properties and Test Methods for Rovene 7007
    PropertyValueTest Method
    Solids content54–56 %Infrared moisture balance, 105 °C
    pH4.0–5.5ISO 976
    Viscosity (LVF, #3, 60 rpm)200–800 mPa·sASTM D2196
    Average particle size250–350 nmDynamic light scattering (Malvern Zetasizer)
    Glass transition temperature (midpoint)34 °CDSC, 10 °C/min, second heat
    Minimum film-forming temperature28 °CMFFT bar, ASTM D2354
    Carboxyl content (as acrylic acid)1.5–2.5 %Potentiometric titration
    In nonwovens and technical textiles, Rovene 7007 can be applied as a self-crosslinking saturant for airlaid and wetlaid webs destined for high-temperature filter media or abrasive backing papers. The absence of formaldehyde-generating crosslinkers aligns with OEKO-TEX Standard 100 Class I requirements for skin-contact articles. Adhesion to polyester fibers, inherently difficult due to low surface energy, improves markedly when the saturant bath includes 0.5 % of an organofunctional silane coupling agent (pre-hydrolyzed gamma-glycidoxypropyltrimethoxysilane) based on binder solids. Nip pressure on a two-roll padder set to 40 PLI and can drying above 135 °C are necessary to overcome the high-Tg polymer’s resistance to flow into fiber interstices. Without sufficient drying temperature, the cured nonwoven exhibits delamination during a Taber abrasion test (ASTM D3884, H-18 wheels, 1,000 g load), losing more than 15 % weight after 200 cycles, compared to less than 5 % when dried at 150 °C.
    Table 2 — Comparative Performance: Rovene 7007 vs. Conventional VAE and Acrylic in Structural Adhesive Application (Crosslinked with 3 % Polyfunctional Aziridine, 2-mil Bondline on Aluminum)
    PropertyRovene 7007Standard VAE (Tg 5 °C)All-Acrylic (Tg 35 °C)Test Method
    Lap shear strength, Al-Al, 25 °C3.8 MPa1.2 MPa4.5 MPaASTM D1002
    Lap shear strength after 7 d water immersion2.9 MPa0.8 MPa3.1 MPaASTM D1002 after ISO 2812-2
    Heat resistance (SAFT, 1 kg static)92 °C48 °C105 °CASTM D4498
    Tensile elongation at break (free film)320 %680 %210 %ASTM D638 (Type V specimen, 50 mm/min)
    The presence of carboxylation modifies the rheological response to alkali-swellable associative thickeners. In contrast to a non-carboxylated VAE, Rovene 7007 exhibits a marked thixotropic loop when neutralized with AMP to pH 8.5 and thickened with a hydrophobically modified alkali-swellable emulsion (HASE) at 1.2 % dry on binder. Controlled stress rheometry (cone-and-plate, 40 mm diameter, angle) reveals a zero-shear viscosity of 12 Pa·s and a shear-thinning index of 0.65 (ratio of viscosity at 100 s⁻¹ to 1 s⁻¹), suitable for roller-applied pressure-sensitive adhesives where a high static yield stress prevents flow after die-cutting. Formulators accustomed to acrylics must adjust block resistance testing protocols: VAE films possess a slightly lower Gardner block resistance (face-to-face, 50 °C, 1 psi, 30 min) than a methyl methacrylate/n-butyl acrylate copolymer of identical Tg, but the difference disappears when a 1.0 % paraffin wax emulsion is post-added, yielding a rating of 8 on the 1–10 scale of ASTM D4946.